Devices

Device Recall Materialise Distributed by Biomet Orthopedics, Signature Personalized Patient Care System

Model / Serial
Lot# 124471
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution to the Netherlands only.
Product Description
Signature TKA GDE/MDL Set 04-05 (Femur & Tibia) || The Signature Patient-Specific Surgical Guides are intended to be used as part of the Signature Personalized Patient Care System. Lt is intended to be used as a guide during the surgical procedure for total and partial knee arthroplasty.
Manufacturer
Materialise N.V.
1 Event
- Recall of Device Recall Materialise Distributed by Biomet Orthopedics, Signature Personalized Patient Care System

Manufacturer

Materialise N.V.

Manufacturer Address
Materialise N.V., 15 Technologielaan, Heverlee Belgium
Manufacturer Parent Company (2017)
Materialise Nv
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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